Lucid Genomics Webinar
🚀 Join the Lucid Webinar: Your Platform for Long-Read and Methylation Analysis
Labs have invested heavily in long-read sequencing platforms — yet turning that data into actionable biological insights remains a major challenge.
🧬 In this webinar, we’ll showcase the latest features of the Lucid Whole Genome Analysis Platform, designed for intuitive, end-to-end analysis of long-read WGS data.
✔️ Seamless integration of methylation data and Differentially Methylated Regions (DMRs)
✔️ Advanced detection and interpretation of structural variants and tandem repeats
✔️ Integrated multi-omics analysis (Hi-C, ChIP-seq, RNA-seq) to accelerate identification of causative pathogenic variants
✔️ Cohort-level insights in seconds — built for real research workflows
Whether you're working in rare disease, complex traits, or translational research, this session will show how to turn long-read data into actionable biological insight.
📅 March 26th
🕓 4 PM CET | 10 AM EST
💻 Online Webinar